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Study identifier: NCT07403084 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Post-market Clinical Follow-up Study of NEMOST V2

Condition: Scoliosis Neuromuscular · Scoliosis Idiopathic · Consent Forms  ·  Sponsor: EUROS

PhaseNA
Planned participants140
Who can joinAll sexes, 5 Years to 17 Years
Healthy volunteersNo

About this study

The NEMOST spinal implant is a growth domino intended for the surgical treatment of progressive scoliosis in children. As part of post-market surveillance, EUROS is conducting a retrospective and prospective study to collect clinical and radiological data on the NEMOST growth domino. Retrospective and prospective multicenter post-market surveillance clinical study. This study is interventional, non-randomized, and uncontrolled. The primary objective of this clinical study is to monitor complications related to the NEMOST growth domino during a 5-year postoperative follow-up in patients treated for progressive scoliosis in children. The secondary objective of this clinical study is to monitor the performance of the NEMOST growth domino during a 5-year postoperative follow-up in patients treated for progressive scoliosis in children. The study will include 140 patients.

This description comes directly from the study's public registry record.

Talk to the study team

Célia Armanet, PHD  ·  +330756848896  ·  carmanet@euros.fr

Always discuss trial participation with your own doctor first.

Locations (5)

Hopital Lenval NiceNice, Provence-Alpes-Côte d'Azur Region, FranceRecruiting
CHU PellegrinBordeaux, FranceRecruiting
Hospices Civils de LyonLyon, FranceNot Yet Recruiting
Hopital Armand TrousseauParis, FranceNot Yet Recruiting
Hopital NeckerParis, FranceNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT07403084